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L-岩藻糖参与了人类肠道微生物组的相互作用。

L-Fucose is involved in human-gut microbiome interactions.

机构信息

Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.

Department of Food Science and Human Nutrition, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.

出版信息

Appl Microbiol Biotechnol. 2023 Jun;107(12):3869-3875. doi: 10.1007/s00253-023-12527-y. Epub 2023 May 6.

Abstract

L-Fucose is one of the key metabolites in human-gut microbiome interactions. It is continuously synthesized by humans in the form of fucosylated glycans and fucosyl-oligosaccharides and delivered into the gut throughout their lifetime. Gut microorganisms metabolize L-fucose and produce short-chain fatty acids, which are absorbed by epithelial cells and used as energy sources or signaling molecules. Recent studies have revealed that the carbon flux in L-fucose metabolism by gut microorganisms is distinct from that in other sugar metabolisms because of cofactor imbalance and low efficiencies in energy synthesis of L-fucose metabolism. The large amounts of short-chain fatty acids produced during microbial L-fucose metabolism are used by epithelial cells to recover most of the energy used up during L-fucose synthesis. In this review, we present a detailed overview of microbial L-fucose metabolism and a potential solution for disease treatment and prevention using genetically engineered probiotics that modulate fucose metabolism. Our review contributes to the understanding of human-gut microbiome interactions through L-fucose metabolism. KEY POINTS: • Fucose-metabolizing microorganisms produce large amounts of short-chain fatty acids • Fucose metabolism differs from other sugar metabolisms by cofactor imbalance • Modulating fucose metabolism is the key to control host-gut microbiome interactions.

摘要

L-岩藻糖是人类肠道微生物组相互作用的关键代谢物之一。它以岩藻糖基化聚糖和岩藻糖寡糖的形式在人体内不断合成,并在其一生中输送到肠道。肠道微生物代谢 L-岩藻糖并产生短链脂肪酸,这些脂肪酸被上皮细胞吸收并用作能量来源或信号分子。最近的研究表明,由于辅助因子失衡和 L-岩藻糖代谢的能量合成效率低下,肠道微生物中 L-岩藻糖代谢的碳通量与其他糖代谢不同。微生物 L-岩藻糖代谢过程中产生的大量短链脂肪酸被上皮细胞用于回收在 L-岩藻糖合成过程中消耗的大部分能量。在这篇综述中,我们详细介绍了微生物 L-岩藻糖代谢,并提出了一种使用基因工程益生菌调节岩藻糖代谢来治疗和预防疾病的潜在解决方案。我们的综述有助于通过 L-岩藻糖代谢来理解人类肠道微生物组的相互作用。关键点:• 代谢岩藻糖的微生物会产生大量的短链脂肪酸• 由于辅助因子失衡,岩藻糖代谢与其他糖代谢不同• 调节岩藻糖代谢是控制宿主-肠道微生物组相互作用的关键。

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